Computational framework for targeted high-coverage sequencing based NIPT

por Teder, Hindrek, Paluoja, Priit, Rekker, Kadri, Salumets, Andres, Krjutškov, Kaarel, Palta, Priit
Publicado 2019

Detection of tmRNA molecules on microarrays at low temperatures using helper oligonucleotides

por Kaplinski, Lauris, Scheler, Ott, Parkel, Sven, Palta, Priit, Toome, Kadri, Kurg, Ants, Remm, Maido
Publicado 2010

Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples

por Paluoja, Priit, Teder, Hindrek, Ardeshirdavani, Amin, Bayindir, Baran, Vermeesch, Joris, Salumets, Andres, Krjutškov, Kaarel, Palta, Priit
Publicado 2021

Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications

por Scheler, Ott, Glynn, Barry, Parkel, Sven, Palta, Priit, Toome, Kadri, Kaplinski, Lauris, Remm, Maido, Maher, Majella, Kurg, Ants
Publicado 2009

A Comparison of the Whole Genome Approach of MeDIP-Seq to the Targeted Approach of the Infinium HumanMethylation450 BeadChip(®) for Methylome Profiling

por Clark, Christine, Palta, Priit, Joyce, Christopher J., Scott, Carol, Grundberg, Elin, Deloukas, Panos, Palotie, Aarno, Coffey, Alison J.
Publicado 2012

Detection of NASBA amplified bacterial tmRNA molecules on SLICSel designed microarray probes

por Scheler, Ott, Kaplinski, Lauris, Glynn, Barry, Palta, Priit, Parkel, Sven, Toome, Kadri, Maher, Majella, Barry, Thomas, Remm, Maido, Kurg, Ants
Publicado 2011

Haplotype Phasing and Inheritance of Copy Number Variants in Nuclear Families

por Palta, Priit, Kaplinski, Lauris, Nagirnaja, Liina, Veidenberg, Andres, Möls, Märt, Nelis, Mari, Esko, Tõnu, Metspalu, Andres, Laan, Maris, Remm, Maido
Publicado 2015

Structural Genomic Variation as Risk Factor for Idiopathic Recurrent Miscarriage

por Nagirnaja, Liina, Palta, Priit, Kasak, Laura, Rull, Kristiina, Christiansen, Ole B, Nielsen, Henriette S, Steffensen, Rudi, Esko, Tõnu, Remm, Maido, Laan, Maris
Publicado 2014

High-resolution population-specific recombination rates and their effect on phasing and genotype imputation

por Hassan, Shabbeer, Surakka, Ida, Taskinen, Marja-Riitta, Salomaa, Veikko, Palotie, Aarno, Wessman, Maija, Tukiainen, Taru, Pirinen, Matti, Palta, Priit, Ripatti, Samuli
Publicado 2020

GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer

por Koel, Mariann, Võsa, Urmo, Jõeloo, Maarja, Läll, Kristi, Gualdo, Natàlia P, Laivuori, Hannele, Lemmelä, Susanna, Daly, Mark, Palta, Priit, Mägi, Reedik, Laisk, Triin
Publicado 2023

Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom

por Chheda, Himanshu, Palta, Priit, Pirinen, Matti, McCarthy, Shane, Walter, Klaudia, Koskinen, Seppo, Salomaa, Veikko, Daly, Mark, Durbin, Richard, Palotie, Aarno, Aittokallio, Tero, Ripatti, Samuli
Publicado 2017

Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel

por Mitt, Mario, Kals, Mart, Pärn, Kalle, Gabriel, Stacey B, Lander, Eric S, Palotie, Aarno, Ripatti, Samuli, Morris, Andrew P, Metspalu, Andres, Esko, Tõnu, Mägi, Reedik, Palta, Priit
Publicado 2017

The role of polygenic risk and susceptibility genes in breast cancer over the course of life

por Mars, Nina, Widén, Elisabeth, Kerminen, Sini, Meretoja, Tuomo, Pirinen, Matti, della Briotta Parolo, Pietro, Palta, Priit, Palotie, Aarno, Kaprio, Jaakko, Joensuu, Heikki, Daly, Mark, Ripatti, Samuli
Publicado 2020

Primary age‐related tauopathy in a Finnish population‐based study of the oldest old (Vantaa 85+)

por Savola, Sara, Kaivola, Karri, Raunio, Anna, Kero, Mia, Mäkelä, Mira, Pärn, Kalle, Palta, Priit, Tanskanen, Maarit, Tuimala, Jarno, Polvikoski, Tuomo, Tienari, Pentti J., Paetau, Anders, Myllykangas, Liisa
Publicado 2022

Targeted gene expression profiling for accurate endometrial receptivity testing

por Meltsov, Alvin, Saare, Merli, Teder, Hindrek, Paluoja, Priit, Arffman, Riikka K., Piltonen, Terhi, Laudanski, Piotr, Wielgoś, Mirosław, Gianaroli, Luca, Koel, Mariann, Peters, Maire, Salumets, Andres, Krjutškov, Kaarel, Palta, Priit
Publicado 2023

TAC-seq: targeted DNA and RNA sequencing for precise biomarker molecule counting

por Teder, Hindrek, Koel, Mariann, Paluoja, Priit, Jatsenko, Tatjana, Rekker, Kadri, Laisk-Podar, Triin, Kukuškina, Viktorija, Velthut-Meikas, Agne, Fjodorova, Olga, Peters, Maire, Kere, Juha, Salumets, Andres, Palta, Priit, Krjutškov, Kaarel
Publicado 2018

NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidies

por Sauk, Martin, Žilina, Olga, Kurg, Ants, Ustav, Eva-Liina, Peters, Maire, Paluoja, Priit, Roost, Anne Mari, Teder, Hindrek, Palta, Priit, Brison, Nathalie, Vermeesch, Joris R., Krjutškov, Kaarel, Salumets, Andres, Kaplinski, Lauris
Publicado 2018

The GENCODE exome: sequencing the complete human exome

por Coffey, Alison J, Kokocinski, Felix, Calafato, Maria S, Scott, Carol E, Palta, Priit, Drury, Eleanor, Joyce, Christopher J, LeProust, Emily M, Harrow, Jen, Hunt, Sarah, Lehesjoki, Anna-Elina, Turner, Daniel J, Hubbard, Tim J, Palotie, Aarno
Publicado 2011

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

por Ripatti, Pietari, Rämö, Joel T., Mars, Nina J., Fu, Yu, Lin, Jake, Söderlund, Sanni, Benner, Christian, Surakka, Ida, Kiiskinen, Tuomo, Havulinna, Aki S., Palta, Priit, Freimer, Nelson B., Widén, Elisabeth, Salomaa, Veikko, Tukiainen, Taru, Pirinen, Matti, Palotie, Aarno, Taskinen, Marja-Riitta, Ripatti, Samuli
Publicado 2020

Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis

por Ruotsalainen, Sanni E., Surakka, Ida, Mars, Nina, Karjalainen, Juha, Kurki, Mitja, Kanai, Masahiro, Krebs, Kristi, Graham, Sarah, Mishra, Pashupati P., Mishra, Binisha H., Sinisalo, Juha, Palta, Priit, Lehtimäki, Terho, Raitakari, Olli, Milani, Lili, Okada, Yukinori, Palotie, Aarno, Widen, Elisabeth, Daly, Mark J., Ripatti, Samuli
Publicado 2022